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https://doi.org/10.1039/c4cc02501f
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Cite Publication Date: Jan 1, 2014 | |
 Citations: 41 |
Affiliation: National Chemical Laboratory
A simple procedure for the synthesis of 2-aroylindole derivatives comprising a one-pot CuI-catalyzed SNAr reaction of o-bromochalcones with sodium azide and subsequent intramolecular cyclization through nitrene C-H insertion has been developed. This protocol is also applicable with the 2'-bromocinnamates giving the indole-2-carboxylates.
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